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rs121913126

From SNPedia

Orientationminus
Stabilizedminus
Make rs121913126(C;C)
Make rs121913126(C;T)
Make rs121913126(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position26773681
GeneGABRB3
is asnp
is mentioned by
dbSNPrs121913126
dbSNP (old)rs121913126
ClinGenrs121913126
ebirs121913126
HLIrs121913126
Exacrs121913126
Gnomadrs121913126
Varsomers121913126
Maprs121913126
PheGenIrs121913126
Biobankrs121913126
1000 genomesrs121913126
hgdprs121913126
ensemblrs121913126
gopubmedrs121913126
geneviewrs121913126
scholarrs121913126
googlers121913126
pharmgkbrs121913126
gwascentralrs121913126
openSNPrs121913126
23andMers121913126
23andMe allrs121913126
SNP Nexus

SNPshotrs121913126
SNPdbers121913126
MSV3drs121913126
GWAS Ctlgrs121913126
Max Magnitude
OMIM137192
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913126(T;T)
Alt rs121913126(T;T)
Reference rs121913126(C;C)
Significance Other
Disease Epilepsy not specified
Variation info
Gene GABRB3
CLNDBN Epilepsy, childhood absence 5 not specified
Reversed 1
HGVS NC_000015.9:g.27018828G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017576.3, RCV000414639.1,